CH658384A5 - Haarfaerbezusammensetzungen. - Google Patents

Haarfaerbezusammensetzungen. Download PDF

Info

Publication number: CH658384A5
Authority: CH; Switzerland
Prior art keywords: hair; formula; dye; coloring; dyes
Prior art date: 1983-04-11

Application number

CH156484A

Other languages

German (de)

English (en)

Inventor

Tadashi Nomura

Toshiyuki Nemoto

Yasuhiro Ikeda

Original Assignee

Kao Corp

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1983-04-11

Filing date

1984-03-28

Publication date

1986-11-14

1984-03-28 Application filed by Kao Corp filed Critical Kao Corp

1986-11-14 Publication of CH658384A5 publication Critical patent/CH658384A5/de

Links

239000000118 hair dye Substances 0.000 claims description 44
239000000203 mixture Substances 0.000 claims description 27
125000000217 alkyl group Chemical group 0.000 claims 3
125000004429 atom Chemical group 0.000 claims 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
125000003545 alkoxy group Chemical group 0.000 claims 1
125000003118 aryl group Chemical group 0.000 claims 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
229910052794 bromium Inorganic materials 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 claims 1
229910052801 chlorine Inorganic materials 0.000 claims 1
239000000460 chlorine Substances 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
239000000975 dye Substances 0.000 description 24
238000004040 coloring Methods 0.000 description 19
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 17
150000001875 compounds Chemical class 0.000 description 14
230000003647 oxidation Effects 0.000 description 13
238000007254 oxidation reaction Methods 0.000 description 13
239000000049 pigment Substances 0.000 description 13
239000000758 substrate Substances 0.000 description 13
-1 3,3 ' -Iminodiphenyl Chemical group 0.000 description 10
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
238000004043 dyeing Methods 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 8
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
230000037308 hair color Effects 0.000 description 7
239000006210 lotion Substances 0.000 description 7
238000000034 method Methods 0.000 description 7
238000002360 preparation method Methods 0.000 description 7
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
239000002952 polymeric resin Substances 0.000 description 5
238000003786 synthesis reaction Methods 0.000 description 5
229920003002 synthetic resin Polymers 0.000 description 5
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
239000000654 additive Substances 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
239000002612 dispersion medium Substances 0.000 description 4
239000000543 intermediate Substances 0.000 description 4
239000007800 oxidant agent Substances 0.000 description 4
239000001024 permanent hair color Substances 0.000 description 4
239000000047 product Substances 0.000 description 4
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 4
239000011734 sodium Substances 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000000126 substance Substances 0.000 description 4
239000001027 temporary hair color Substances 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 3
239000003086 colorant Substances 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
239000006071 cream Substances 0.000 description 3
238000009472 formulation Methods 0.000 description 3
239000007789 gas Substances 0.000 description 3
229910052742 iron Inorganic materials 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
239000003607 modifier Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 2
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 2
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
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101150065749 Churc1 gene Proteins 0.000 description 2
229910002621 H2PtCl6 Inorganic materials 0.000 description 2
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XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
102100038239 Protein Churchill Human genes 0.000 description 2
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
239000002280 amphoteric surfactant Substances 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
239000003945 anionic surfactant Substances 0.000 description 2
229920006317 cationic polymer Polymers 0.000 description 2
239000003093 cationic surfactant Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
239000006103 coloring component Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
238000004821 distillation Methods 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
239000000284 extract Substances 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
239000003205 fragrance Substances 0.000 description 2
235000011187 glycerol Nutrition 0.000 description 2
239000003906 humectant Substances 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
229940057995 liquid paraffin Drugs 0.000 description 2
150000002739 metals Chemical class 0.000 description 2
239000002736 nonionic surfactant Substances 0.000 description 2
230000001590 oxidative effect Effects 0.000 description 2
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
229940079877 pyrogallol Drugs 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
239000001026 semi permanent hair color Substances 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
238000012360 testing method Methods 0.000 description 2
PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 1
LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
ZBTRTXLGWIKSMO-UHFFFAOYSA-N (4-aminophenyl)sulfamic acid Chemical compound NC1=CC=C(NS(O)(=O)=O)C=C1 ZBTRTXLGWIKSMO-UHFFFAOYSA-N 0.000 description 1
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 description 1
HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 description 1
BAHPQISAXRFLCL-UHFFFAOYSA-N 2,4-Diaminoanisole Chemical compound COC1=CC=C(N)C=C1N BAHPQISAXRFLCL-UHFFFAOYSA-N 0.000 description 1
VLZVIIYRNMWPSN-UHFFFAOYSA-N 2-Amino-4-nitrophenol Chemical compound NC1=CC([N+]([O-])=O)=CC=C1O VLZVIIYRNMWPSN-UHFFFAOYSA-N 0.000 description 1
DOPJTDJKZNWLRB-UHFFFAOYSA-N 2-Amino-5-nitrophenol Chemical compound NC1=CC=C([N+]([O-])=O)C=C1O DOPJTDJKZNWLRB-UHFFFAOYSA-N 0.000 description 1
FECNOIODIVNEKI-UHFFFAOYSA-N 2-[(2-aminobenzoyl)amino]benzoic acid Chemical class NC1=CC=CC=C1C(=O)NC1=CC=CC=C1C(O)=O FECNOIODIVNEKI-UHFFFAOYSA-N 0.000 description 1
MGLZGLAFFOMWPB-UHFFFAOYSA-N 2-chloro-1,4-phenylenediamine Chemical compound NC1=CC=C(N)C(Cl)=C1 MGLZGLAFFOMWPB-UHFFFAOYSA-N 0.000 description 1
OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 1
RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
HVHNMNGARPCGGD-UHFFFAOYSA-N 2-nitro-p-phenylenediamine Chemical compound NC1=CC=C(N)C([N+]([O-])=O)=C1 HVHNMNGARPCGGD-UHFFFAOYSA-N 0.000 description 1
BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
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WHODQVWERNSQEO-UHFFFAOYSA-N 4-Amino-2-nitrophenol Chemical compound NC1=CC=C(O)C([N+]([O-])=O)=C1 WHODQVWERNSQEO-UHFFFAOYSA-N 0.000 description 1
BXIXXXYDDJVHDL-UHFFFAOYSA-N 4-Chloro-ortho-phenylenediamine Chemical compound NC1=CC=C(Cl)C=C1N BXIXXXYDDJVHDL-UHFFFAOYSA-N 0.000 description 1
HDGMAACKJSBLMW-UHFFFAOYSA-N 4-amino-2-methylphenol Chemical compound CC1=CC(N)=CC=C1O HDGMAACKJSBLMW-UHFFFAOYSA-N 0.000 description 1
HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 description 1
DGRGLKZMKWPMOH-UHFFFAOYSA-N 4-methylbenzene-1,2-diamine Chemical compound CC1=CC=C(N)C(N)=C1 DGRGLKZMKWPMOH-UHFFFAOYSA-N 0.000 description 1
QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 description 1
RAUWPNXIALNKQM-UHFFFAOYSA-N 4-nitro-1,2-phenylenediamine Chemical compound NC1=CC=C([N+]([O-])=O)C=C1N RAUWPNXIALNKQM-UHFFFAOYSA-N 0.000 description 1
GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
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GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
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ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
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102000011782 Keratins Human genes 0.000 description 1
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244000208060 Lawsonia inermis Species 0.000 description 1
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239000004698 Polyethylene Substances 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
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239000004115 Sodium Silicate Substances 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
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RJUVPCYAOBNZAX-VOTSOKGWSA-N ethyl (e)-3-(dimethylamino)-2-methylprop-2-enoate Chemical compound CCOC(=O)C(\C)=C\N(C)C RJUVPCYAOBNZAX-VOTSOKGWSA-N 0.000 description 1
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230000003700 hair damage Effects 0.000 description 1
UBHWBODXJBSFLH-UHFFFAOYSA-N hexadecan-1-ol;octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO.CCCCCCCCCCCCCCCCCCO UBHWBODXJBSFLH-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
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239000004615 ingredient Substances 0.000 description 1
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229940039717 lanolin Drugs 0.000 description 1
235000019388 lanolin Nutrition 0.000 description 1
239000011133 lead Substances 0.000 description 1
QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229940018564 m-phenylenediamine Drugs 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
239000001005 nitro dye Substances 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
239000002357 osmotic agent Substances 0.000 description 1
ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
239000002304 perfume Substances 0.000 description 1
235000019271 petrolatum Nutrition 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
229960001553 phloroglucinol Drugs 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
229910052697 platinum Inorganic materials 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
239000003380 propellant Substances 0.000 description 1
VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
239000002453 shampoo Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
229940037001 sodium edetate Drugs 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
229940045872 sodium percarbonate Drugs 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000004071 soot Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
239000001017 thiazole dye Substances 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
235000015961 tonic Nutrition 0.000 description 1
230000001256 tonic effect Effects 0.000 description 1
229960000716 tonics Drugs 0.000 description 1
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
235000020234 walnut Nutrition 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
- A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Birds (AREA)
Epidemiology (AREA)
Cosmetics (AREA)
Compositions Of Macromolecular Compounds (AREA)

CH156484A 1983-04-11 1984-03-28 Haarfaerbezusammensetzungen. CH658384A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP6346783A JPS59190910A (ja)	1983-04-11	1983-04-11	染毛剤組成物

Publications (1)

Publication Number	Publication Date
CH658384A5 true CH658384A5 (de)	1986-11-14

Family

ID=13230068

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH156484A CH658384A5 (de)	1983-04-11	1984-03-28	Haarfaerbezusammensetzungen.

Country Status (6)

Country	Link
JP (1)	JPS59190910A (ja)
AT (1)	AT393450B (ja)
CH (1)	CH658384A5 (ja)
DE (1)	DE3413125A1 (ja)
GB (1)	GB2138845B (ja)
HK (1)	HK43990A (ja)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1290105C (en) *	1986-02-26	1991-10-08	Petrina Felicity Fridd	Colouring keratinous material
GB2186889A (en) *	1986-02-26	1987-08-26	Dow Corning	Colouring keratinous material
GB8618634D0 (en) *	1986-07-30	1986-09-10	Unilever Plc	Treatment of keratinous fibres
LU86899A1 (fr) *	1987-05-25	1989-01-19	Oreal	Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes a un iodure et composition tinctoriale mise en oeuvre
FR2624873B1 (fr) *	1987-12-18	1992-01-10	Rhone Poulenc Chimie	Particules composites magnetisables a base d'organopolysiloxane reticule, leur procede de preparation et leur application en biologie
JPH0474113A (ja) *	1990-07-13	1992-03-09	Kao Corp	染毛剤組成物
DE69219710T2 (de) *	1991-02-15	1998-01-22	Shiseido Co Ltd	Saures haarfärbemittel
JPH05194161A (ja) *	1991-08-20	1993-08-03	Shiseido Co Ltd	頭髪用酸性染毛料組成物
US5281240A (en) *	1992-09-21	1994-01-25	Dow Corning Corporation	Method of coloring hair with water soluble acid dyes
DE4443062C2 (de) *	1994-12-03	1997-07-17	Wella Ag	Mittel und Verfahren zur dauerhaften Haarverformung
FR2769218B1 (fr) *	1997-10-03	2000-03-10	Oreal	Composition oxydante et utilisations pour la teinture, pour la deformation permanente ou pour la decoloration des fibres keratiniques
FR2783416B1 (fr)	1998-08-26	2002-05-03	Oreal	Composition de teinture pour fibres keratiniques avec un colorant direct cationique et une silicone
JP2002193769A (ja)	2000-12-26	2002-07-10	Dow Corning Toray Silicone Co Ltd	酸化染毛剤組成物
FR2831808B1 (fr) *	2001-11-08	2003-12-19	Oreal	Composition de teinture pour fibres keratiniques comprenant une silicone aminee particuliere
FR2831807B1 (fr) *	2001-11-08	2004-10-01	Oreal	Composition de teinture pour fibres keratiniques comprenant une silicone aminee particuliere
KR20040007097A (ko) *	2002-07-16	2004-01-24	주식회사 엘지생활건강	염모제 및 염색 후처리제 조성물
DE10304923A1 (de) *	2003-02-07	2004-08-26	Ge Bayer Silicones Gmbh & Co. Kg	Herstellung und Verwendung Polyamino- und/oder Polyammonium-Polysiloxancopolymere enthaltender Formulierungen
ATE424806T1 (de)	2003-12-18	2009-03-15	Procter & Gamble	Erhöhung der farbwahrnehmung künstlich gefärbter haare
FR2910282B1 (fr) *	2006-12-21	2009-06-05	Oreal	Composition de teinture directe comprenant un tensio-actif cationique, un bioheteropolysaccharide, un tensio-actif amphotere ou non ionique et un colorant direct
DE102019218232A1 (de) *	2019-11-26	2021-05-27	Henkel Ag & Co. Kgaa	Verbesserung der Leistung von auf Pigmenten basierenden Färbemitteln durch Anwendung eines Vorbehandlungsmittels
DE102019218236A1 (de) *	2019-11-26	2021-05-27	Henkel Ag & Co. Kgaa	Verfahren zur Verbesserung des Griffgefühls von gefärbtem keratinischem Material, insbesondere menschlichen Haaren

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR1585308A (ja) *	1967-10-10	1970-01-16
JPS49117492U (ja) *	1973-02-06	1974-10-07
GB1524683A (en) *	1974-12-20	1978-09-13	Bicc Ltd	Termination of electric cables
US4096243A (en) *	1976-02-09	1978-06-20	Clairol Incorporated	Composition for lightening hair containing an oxidizing agent and certain quaternary amines
FR2443476A1 (fr) *	1978-12-05	1980-07-04	Oreal	Nouveaux polysiloxanes tensioactifs, procede pour les preparer et compositions les contenant
JPS57192310A (en) *	1981-05-20	1982-11-26	Kao Corp	Hair dyeing agent composition

1983
- 1983-04-11 JP JP6346783A patent/JPS59190910A/ja active Granted
1984
- 1984-02-22 GB GB08404625A patent/GB2138845B/en not_active Expired
- 1984-03-20 AT AT94084A patent/AT393450B/de not_active IP Right Cessation
- 1984-03-28 CH CH156484A patent/CH658384A5/de not_active IP Right Cessation
- 1984-04-06 DE DE19843413125 patent/DE3413125A1/de not_active Ceased
1990
- 1990-06-07 HK HK43990A patent/HK43990A/xx unknown

Also Published As

Publication number	Publication date
AT393450B (de)	1991-10-25
GB2138845B (en)	1986-03-19
ATA94084A (de)	1991-04-15
GB2138845A (en)	1984-10-31
DE3413125A1 (de)	1984-10-11
JPS59190910A (ja)	1984-10-29
HK43990A (en)	1990-06-15
JPH0363528B2 (ja)	1991-10-01
GB8404625D0 (en)	1984-03-28

Legal Events

Date	Code	Title	Description
1996-11-15	PL	Patent ceased

Publication	Publication Date	Title
CH658384A5 (de)	1986-11-14	Haarfaerbezusammensetzungen.
EP0277996B1 (de)	1991-10-09	Mittel zum oxidativen färben von haaren, verfahren zu seiner herstellung und verwendung des mittels
DE69412374T2 (de)	1999-05-06	Naphthol-Kuppler
DE68904942T2 (de)	1993-06-03	Mindestens eine doppelte und eine einfache farbbase enthaltendes oxidationsfaerbemittel und verfahren zur faerbung mit diesem mittel.
WO1993009759A1 (de)	1993-05-27	5,6-dihydroxyindoline als additiv zu haarfärberezepturen
WO1992004883A1 (de)	1992-04-02	Haarfärbemittel
EP1037591A1 (de)	2000-09-27	Kosmetische mittel enthaltend eine spezielle wirkstoffkombination
EP0727203A1 (de)	1996-08-21	Oxidationshaarfärbemittel
EP0460128B1 (de)	1993-06-09	Mittel und verfahren zum oxidativen färben von haaren
WO1980000417A1 (fr)	1980-03-20	Preparation permettant la coloration des cheveux
EP0491003A1 (de)	1992-06-24	Egalisierende oxidationshaarfärbemittel.
DE3131366C2 (ja)	1987-11-05
EP0765154B1 (de)	1999-01-20	Direktziehendes haarfärbemittel
EP0289782B1 (de)	1992-03-04	Verwendung von 2,6-Dinitro-anilinderivaten in Haarfärbemitteln und neue 2,6-Dinitro-anilinderivate
EP0150765B1 (de)	1989-03-22	Verwendung von p-Ureidoalkylamino-nitrobenzolverbindungen in Haarfärbemitteln und neue p-Ureidoalkylamino-nitrobenzolverbindungen
EP0895471A1 (de)	1999-02-10	Färbemittel zur färbung von keratinischen fasern
WO1995017877A1 (de)	1995-07-06	Verwendung von allylaminophenolen in oxidationsfärbemitteln
EP0012965B1 (de)	1982-08-25	Mittel und Verfahren zur Färbung von Haaren
DE2812678A1 (de)	1979-10-04	Haarfaerbemittel
EP0896519B1 (de)	2003-04-09	Färbemittel zur färbung von keratinischen fasern
EP0881894B1 (de)	2002-10-30	Färbemittel zur färbung von keratinischen fasern
DE4305258A1 (de)	1994-09-01	Verwendung von 1,8-Dihydroxynaphthalinen als Oxidationsfarbstoffvorprodukte in Oxidationsfärbemitteln
EP0874615A1 (de)	1998-11-04	Färbemittel zur färbung von keratinischen fasern
DE3508309A1 (de)	1986-09-11	Haarfaerbemittel
EP0348849A1 (de)	1990-01-03	Haarfärbemittel